PGT-M conditions
This table shows all PGT-M conditions currently approved and awaiting consideration by the HFEA.
Please note that we are updating this database, and some approved conditions may not be displayed. If you are unsure if a condition has been approved or not, please contact pgtm@hfea.gov.uk.
Download full approved condition list.
| Condition name | Status | OMIM number | Documents |
|---|---|---|---|
| Glycogen Storage Disease Type 4, (GSD4) | approved | 232500 | |
| Glycogen Storage Disease Type Ia | approved | 232200 | |
| Glycogen storage disease V (GSD5) | approved | 232600 | |
| Glycogen storage disease VI (GSD6) | approved | 232700 | |
| Glycogen storage disease VII (GSD7) | approved | 232800 | |
| Goiter, Multinodular 1, with or without Sertoli-Leydig cell tumours (MNG1) | approved | 138800 | |
| Gonadal mosaicism | approved | ||
| Gorlin Syndrome | approved | 109400 | |
| Greig Cephalopolysyndactyly (GCPS) | approved | 175700 | |
| GRN-related Frontotemporal Lobar Degeneration with TDP43 inclusions | approved | 607485 | |
| Haemoglobin SC disease | approved | 141900.0038 | |
| Haemophilia A (HEMA) | approved | 306700 | |
| Haemophilia B (HEMB) | approved | 306900 | |
| Hajdu-Cheney Syndrome (HJCYS) | approved | 102500 | |
| HAJDU-CHENEY SYNDROME; HJCYS | awaiting approval | 102500 | |
| Harel-Yoon Syndrome, (HAYOS) | approved | 617183 | |
| Heimler Syndrome 1 | approved | 234580 | |
| Heimler Syndrome 2 | approved | 616617 | |
| Hereditary Angioedema (HAE) Type I & Type II | approved | 106100 | |
| Hereditary Angioedema (HAE) Type III | approved | 610618 | |